Rare case of Neonatal Lamellar Ichthyosis - Collodian baby

Bangal, Vidyadhar B; Gangapurwala, Sonika; Gavhane, Satyajit P.; Gupta, Kanika

doi:10.7439/ijbar.v5i2.665

Int J of Biomed & Adv Res

2014

DOI: 10.7439/ijbar.v5i2.665

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Rare case of Neonatal Lamellar Ichthyosis - Collodian baby

Vidyadhar B Bangal¹,

Sonika Gangapurwala²,

Satyajit P. Gavhane³

et al.

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2022

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Collodion Ichthyosis With Trisomy – 21: A Case Report

Pal¹

2022

Global Journal for Research Analysis

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Collodion Ichthyosis is a rare disorder presenting at birth with visible scaling/ hyperkeartosis of the skin. The severity of ichthyosis and expression of associated features may be variable. The ichthyosis is known as Mendelian Disorder of cornication (MeDOC). Inborn types have different genetic background like Autosomal Dominant (AD), Autosomal Recessive (AR) and X – linked inheritance. [1] Collodion baby is a very rare form of skin disorder with an estimated incidence of 1 in 50,000 to 100,000 birth. [2] The mortality rate is around 11% in early life due to Dehydration, Electrolyte Imbalance, Sepsis because of severe skin damage. [3, 4]

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Collodion Ichthyosis With Trisomy – 21: A Case Report

Pal¹

2022

Global Journal for Research Analysis

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Rare case of Neonatal Lamellar Ichthyosis - Collodian baby

Cited by 1 publication

References 4 publications

Collodion Ichthyosis With Trisomy – 21: A Case Report

Collodion Ichthyosis With Trisomy – 21: A Case Report

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